Canonical Allele Identifier: CA383651980

Gene: ADIPOR2

Linked Data

• gnomAD v4: 12-1780456-G-A
• MyVariant Identifiers: chr12:g.1889622G>A (hg19) ; chr12:g.1780456G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1780456G>A , CM000674.2:g.1780456G>A	GRCh38
NC_000012.11:g.1889622G>A , CM000674.1:g.1889622G>A	GRCh37
NC_000012.10:g.1759883G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.469G>A MANE Select	ENSP00000349616.4:p.Val157Ile
ENST00000357103.4:c.469G>A	ENSP00000349616.4:p.Val157Ile
ENST00000535774.1:n.426G>A
ENST00000537190.1:n.309G>A
NM_024551.2:c.469G>A	NP_078827.2:p.Val157Ile
XM_005253789.1:c.469G>A	XP_005253846.1:p.Val157Ile
XM_006719018.1:c.469G>A	XP_006719081.1:p.Val157Ile
XM_011521024.1:c.469G>A	XP_011519326.1:p.Val157Ile
XM_011521025.1:c.463+2431G>A	XP_011519327.1:n.463+2431G>A
XM_005253789.2:c.469G>A	XP_005253846.1:p.Val157Ile
XM_006719018.2:c.469G>A	XP_006719081.1:p.Val157Ile
XM_011521024.2:c.469G>A	XP_011519326.1:p.Val157Ile
NM_024551.3:c.469G>A MANE Select	NP_078827.2:p.Val157Ile
NM_001375363.1:c.469G>A	NP_001362292.1:p.Val157Ile
NM_001375364.1:c.469G>A	NP_001362293.1:p.Val157Ile
NM_001375365.1:c.469G>A	NP_001362294.1:p.Val157Ile